@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1166496.RAu3Xu2vNbCbWeywindQgnZkcrFnqU7-j94ThfqtNFfG0130_head { this: np:hasAssertion dgn-np:NP1166496.RAu3Xu2vNbCbWeywindQgnZkcrFnqU7-j94ThfqtNFfG0130_assertion; np:hasProvenance dgn-np:NP1166496.RAu3Xu2vNbCbWeywindQgnZkcrFnqU7-j94ThfqtNFfG0130_provenance; np:hasPublicationInfo dgn-np:NP1166496.RAu3Xu2vNbCbWeywindQgnZkcrFnqU7-j94ThfqtNFfG0130_publicationInfo; a np:Nanopublication . dgn-np:NP1166496.RAu3Xu2vNbCbWeywindQgnZkcrFnqU7-j94ThfqtNFfG0130_assertion a np:Assertion . dgn-np:NP1166496.RAu3Xu2vNbCbWeywindQgnZkcrFnqU7-j94ThfqtNFfG0130_provenance a np:Provenance . dgn-np:NP1166496.RAu3Xu2vNbCbWeywindQgnZkcrFnqU7-j94ThfqtNFfG0130_publicationInfo a np:PublicationInfo . } dgn-np:NP1166496.RAu3Xu2vNbCbWeywindQgnZkcrFnqU7-j94ThfqtNFfG0130_assertion { miriam-gene:1956 a ncit:C16612 . lld:C0007131 a ncit:C7057 . dgn-gda:DGNa25d87bb4dc87fc201f38e0c095b77e5 sio:SIO_000628 miriam-gene:1956, lld:C0007131; a sio:SIO_001121 . } dgn-np:NP1166496.RAu3Xu2vNbCbWeywindQgnZkcrFnqU7-j94ThfqtNFfG0130_provenance { dgn-np:NP1166496.RAu3Xu2vNbCbWeywindQgnZkcrFnqU7-j94ThfqtNFfG0130_assertion dcterms:description "[However, a large number of somatic mutations in such protein have been observed to cause drug resistance or sensitivity during pathological progression, limiting the application of reversible EGFR tyrosine kinase inhibitor therapy in NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:24658966; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1166496.RAu3Xu2vNbCbWeywindQgnZkcrFnqU7-j94ThfqtNFfG0130_publicationInfo { this: dcterms:created "2016-05-13T12:50:34+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }